Smart Clinical Trial solution introduction
Optimising clinical trial lifecycle to enable faster drug development
HCLTech’s Smart Clinical Trial (SCT) solution by HCLTech aims to make clinical trials smarter, faster, and more optimized by accelerating the discovery-to-market journey for a drug.
Pharmaceutical companies continually look at adopting faster and effective drug-development models to address competition, consolidation, effective safety-monitoring and management of patient recruitment and retention issues during trials. This healthcare solution allows all stakeholders involved in the clinical trial management system for a drug. They can leverage the Internet of Things (IoT) technology and perform ‘day-to-day’ safety monitoring of the patients participating in the trial/program, thereby boosting protocol adherence and REMS compliance.
This helps in the early identification of trends/patterns contributing to the enhancement in decision-making capabilities for the trial’s outcome, and save time, effort, and capital for the companies. By enabling e-visits through various smart devices to capture vital signs and e-diary data of trial subjects apart from scheduled visits, the solution helps an investigator/clinician to view patient data in real-time by leveraging the smart ‘Patient Portal.’ It also provides safety monitoring and care through multi-disciplinary teams, effectively and immediately. Thus the clinical trial solution helps improve patient safety, faster completion, and compliance with regulatory demands.

SCT Features
Transforming business into next-gen enterprises with industry leading solutions and capabilities

E-visits
Vital signs and e-diary data of study subjects, or patients is collected through smartphone/tablet/Mi-Fi, and smart biometric devices continually between scheduled EDC physical visits

Real-time feedback generation
The smart ‘Patient Portal’ interprets the reading and sends pre-programmable feedback to study subjects

Real-time alerts
An investigator/clinician gets an alert on any abnormal reading to provide safety monitoring and care, effectively and in real-time

Secure, accurate, and complete data recording
Vital signs and e-diary data of the study on the subjects are recorded securely without any human error. They can be sent to the sponsor to be loaded in CDMS or EMR as per extraction protocol
SCT Benefits
Take advantage of the next-gen business drivers that redefine the clinical trial journey


Improve patient safety
- Data reliability and access
- Real-time patient safety monitoring and intervention
- Better mitigation of BIMO, RiskMAPs, and REMS


Faster completion of clinical trials
- Adaptive protocol design
- Flexible washout, run-in, and titration protocols
- The early ID of low dose, placebo, and non-responders
- Reduced patient dropout rate and trial duration
- Improved statistical analysis and IRB decision


Meet regulatory demands
- Improved compliance to protocol
- Generate better and reliable outcomes
- Obtain reliable patient-reported data
Solution architecture
Leveraging the IoT foundation infrastructure to unlock benefits and opportunities


Why HCLTech?
Unmatched Capabilities Expanding New Horizons In IoT
Resources
Explore Our IoT Capabilities And Discover New Business Insights
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